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. 2020 Nov 30;128(11):117009. doi: 10.1289/EHP7255

Figure 1.

Figures 1A, 1B, 1C, and 1E are clustered bar graphs, plotting blood glucose (milligram per deciliter), ranging from 0 to 800 in increments of 200, plasma insulin (micro units per milliliter), ranging from 0 to 400 in increments of 100, homeostatic model assessment of insulin resistance, ranging from 0 to 400 in increments of 100, and blood glucose area under the curve, ranging from 0 to 80000 in increments of 10,000 (y-axis), respectively, across air and ozone (x-axis) for uppercase C 57 black 6, uppercase K K, and uppercase K K A y. Figure 1D is a line graph, plotting blood glucose (milligram per deciliter), ranging from 0 to 500 in increments of 100 (y-axis) across time after Intravenous insulin (minutes), ranging from 0 to 140 in increments of 20 (x-axis) for uppercase C 57 black 6 after air, uppercase K K after air, uppercase K K A y after air, uppercase C 57 black 6 after ozone, uppercase K K after ozone, and uppercase K K Ay after ozone.

Serum glucose and insulin in fasted mice and following an insulin tolerance test (ITT) in C57BL/6J, KK and KKAy mice after air or O3 exposure for 13 d. Plasma concentrations of glucose (A) and insulin (B) were measured from fasted all mice at the time of necropsy, approximately 22 h after the last O3 exposure. Data of plasma glucose and insulin were used to calculate HOMA-IR (C). Time-dependent changes in blood glucose after a bolus insulin challenge in fasted mice were measured from 15 to 130 min after challenge (D). Effects of O3 exposure within each strain and timepoint were determined. For each experimental group the area under the curve (AUC) was calculated between 0 to 130 min using the trapezoid rule (GraphPad Prism, San Diego, CA) (E). Data are expressed as mean±SEM (n=78/group). For Figure 1D: (a) shows significant difference between air- and O3-exposed C57BL/6 mice; (b) shows significant difference between air- and O3-exposed KK mice. (c) shows significant difference between air- and O3-exposed KKAy mice. For remaining figures: (a) significantly different from similarly exposed C57BL/6 mice (b) significantly different from similarly exposed KK mice; (c) significantly different from air-exposed mice of the same strain. Note: Significant differences between indicated groups, p<0.05, were determined using a completely randomized analysis of variance, with factors of time and exposure for the temporal responses in the insulin tolerance test, and with factors of mouse strain and exposure for remaining data. Comparisons of group means were made with the Student–Newman–Keuls post hoc test. Summary data for panels A, B, C, D, and E can be found in Tables S4, S5, S6, S9, and S10, respectively.